Willow Birch Pharma, Inc

FDA inspection history in Taylor, Mississippi, 2016 to 2024

2
Form 483s

Every document, by year

  • Form 483

2016: one Form 483; 2024: one Form 483.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2016One Form 483, at Taylor, Mississippi.
  2. 2016The longest 483 on file: 6 observations over 4 pages at Taylor, Mississippi.
  3. 2024One Form 483, at Taylor, Mississippi.

Cited most

Across all Willow Birch Pharma observations on file

The complete Willow Birch Pharma file.

All 2 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.

$198

The price of the documents, added to your cart together

Sites

Documents

2 on file, newest first
DateDocumentPrice
2024-05-03483 Form 483$99
2016-10-28483 Form 483$99

FEI number 3009864247 · most recent document May 3, 2024

About Willow Birch Pharma, Inc

How many FDA Form 483s has Willow Birch Pharma, Inc received?

FDA Intel has 2 Form 483s on file for Willow Birch Pharma, Inc; the most recent is dated May 3, 2024.

When was Willow Birch Pharma, Inc last inspected by FDA?

The most recent FDA inspection document on file for Willow Birch Pharma, Inc is a Form 483 dated May 3, 2024, for the site in Taylor, Mississippi.

What did FDA cite at Willow Birch Pharma, Inc?

The regulations cited most in the observations on file for Willow Birch Pharma, Inc are 21 CFR 211.188(a) (Batch production and control records), 2 times; 21 CFR 211.130 (Packaging and labeling operations), 1 time; 21 CFR 211.150(b) (Distribution procedures), 1 time.